FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 2232658 · Received July 19, 2011

Report

Report Number
1824206-2011-03800
Event Type
Malfunction
Date Received
July 19, 2011
Date of Event
June 22, 2011
Report Date
June 22, 2011
Manufacturer
HILL-ROM INC
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ADJUSTED THE SIDERAIL LATCH PLATE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE LEFT SIDERAIL WILL NOT LATCH DUE TO A BENT LATCH COVER PLATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BARIATRIC AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1840

Patients

Seq Age Sex Outcome Treatment
1 UNK